共 21 条
[1]
Shapiro, The management of pain in sickle cell disease, Pediatr Clin North Am, 36, pp. 1029-1045, (1989)
[2]
Platt, Thorington, Brambilla, Et al., Pain in sickle cell disease: rates and risk factors, N Engl J Med, 325, pp. 11-16, (1991)
[3]
Vichinsky, Johnson, Lubin, Multidisciplinary approach to pain management in sickle cell disease, Am J Pediat Hematol Oncol, 4, pp. 328-333, (1982)
[4]
Powars, Chan, Is sickle cell crisis a valid measure of clinical severity in sickle cell anemia?, Pathophysiological Aspects of Sickle Cell Vaso-occlusion, 240, pp. 393-402, (1987)
[5]
Gilbert, The health insurance plight of subjects with sickle cell anemia, J Nat Med Assoc, 78, pp. 663-665, (1986)
[6]
Farber, Koshy, Kinney, Et al., Cooperative study of sickle cell disease: Demographic and socioeconomic characteristics of subjects and families with sickle cell disease, J Chron Dis, 38, pp. 495-505, (1985)
[7]
Barrett, Wizotzek, Abel, Et al., Assessment of psychosocial functioning in subjects with sickle cell disease, South Med J, 81, pp. 745-750, (1988)
[8]
Brown, Armstrong, Eckman, Neurocognitive aspects of pediatric sickle cell disease, J Learning Disabilities, 26, pp. 33-45, (1993)
[9]
Lemanek, Moore, Gresham, Et al., Psychological adjustment of children with sickle cell anemia, J Pediatr Psychol, 11, pp. 397-410, (1986)
[10]
Hafner-Eaton, Physician utilization disparities between the uninsured and insured: Comparisons of the chronically ill, acutely ill and well nonelderly populations, JAMA, 269, pp. 787-792, (1993)